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巨噬细胞特异性分子:在分化和激活中的作用

Macrophage-restricted molecules: role in differentiation and activation.

作者信息

Gordon S

机构信息

Sir William Dunn School of Pathology, University of Oxford, UK.

出版信息

Immunol Lett. 1999 Jan;65(1-2):5-8. doi: 10.1016/s0165-2478(98)00116-3.

Abstract

Membrane antigens serve as excellent markers of murine macrophage (MO) differentiation in vivo and in vitro, and have yielded insights into novel MO functions in innate and acquired immunity. We review briefly the use of a range of monoclonal antibodies against MO which show restricted expression: F4/80, macrosialin and sialoadhesin. Differential display PCR strategies have made it possible to identify a novel MO-restricted membrane molecule, a murine MO C-type lectin (mMCL). The isolation of functionally active ab against known receptors such as the scavenger receptor, Class A (SR-A) has provided a key reagent to characterise the role of this molecule in adhesion, endocytosis, phagocytosis and in the regulation of cellular immunity. Studies in SR-A ko mice challenged with BCG and LPS show that the SR-A molecule helps to limit excessive production of cytokines such as TNFalpha by MO that have been activated by infection, and thus protects the host against septic shock.

摘要

膜抗原是体内外小鼠巨噬细胞(MO)分化的优良标志物,并为深入了解其在固有免疫和获得性免疫中的新功能提供了线索。我们简要回顾了一系列针对MO的单克隆抗体的应用,这些抗体呈现限制性表达:F4/80、巨噬唾液酸蛋白和唾液酸黏附素。差异显示PCR策略使得鉴定一种新型的MO限制性膜分子——小鼠MO C型凝集素(mMCL)成为可能。针对已知受体(如A类清道夫受体(SR-A))的功能性活性抗体的分离,为表征该分子在黏附、内吞作用、吞噬作用以及细胞免疫调节中的作用提供了关键试剂。对用卡介苗和脂多糖攻击的SR-A基因敲除小鼠的研究表明,SR-A分子有助于限制被感染激活的MO过度产生细胞因子(如TNFα),从而保护宿主免受败血症性休克。

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